EP0354501A3 - Amino-mono or amino-di[(poly-n-butoxy)-n-butyl amino]-(poly-n-butoxy)-n-butyl amines - Google Patents

Amino-mono or amino-di[(poly-n-butoxy)-n-butyl amino]-(poly-n-butoxy)-n-butyl amines Download PDF

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Publication number
EP0354501A3
EP0354501A3 EP19890114498 EP89114498A EP0354501A3 EP 0354501 A3 EP0354501 A3 EP 0354501A3 EP 19890114498 EP19890114498 EP 19890114498 EP 89114498 A EP89114498 A EP 89114498A EP 0354501 A3 EP0354501 A3 EP 0354501A3
Authority
EP
European Patent Office
Prior art keywords
amino
butoxy
poly
butyl
mono
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP19890114498
Other languages
German (de)
French (fr)
Other versions
EP0354501A2 (en
Inventor
Willibald Dr. Schoenleben
Herbert Dr. Mueller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP0354501A2 publication Critical patent/EP0354501A2/en
Publication of EP0354501A3 publication Critical patent/EP0354501A3/en
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/321Polymers modified by chemical after-treatment with inorganic compounds
    • C08G65/325Polymers modified by chemical after-treatment with inorganic compounds containing nitrogen
    • C08G65/3255Ammonia
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/321Polymers modified by chemical after-treatment with inorganic compounds
    • C08G65/322Polymers modified by chemical after-treatment with inorganic compounds containing hydrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polyethers (AREA)

Abstract

Amino-mono- oder -di[(poly-n-butoxy)-n-butylamino]-(poly-n-butoxy)-n-­ butylamine der allgemeinen Formel I
H₂N-[(CH₂CH₂CH₂CH₂O)x-(CH₂)₄-NH]y-(CH₂CH₂CH₂CH₂O)x-(CH₂)₄-NH₂      (I),
in der x 1 bis 150 und y 1 oder 2 bedeuten, sowie ein Verfahren zur Her­ stellung dieser Verbindungen, in dem man Hydroxy-(poly-n-butoxy)-butanole der allgemeinen Formel II
HO-(CH₂CH₂CH₂CH₂O)x-(CH₂)₄-OH      (II),
in der x 1 bis 150 bedeutet, mit 1,01 bis 300 Moläquivalenten Ammoniak pro Hydroxygruppe in Gegenwart eines Hydrier-/Dehydrierkatalysators und Wasserstoff bei Temperaturen von 150 bis 300°C und Drücken von 20 bis 400 bar umsetzt.
Amino-mono- or -di [(poly-n-butoxy) -n-butylamino] - (poly-n-butoxy) -n-butylamines of the general formula I
H₂N - [(CH₂CH₂CH₂CH₂O) x - (CH₂) ₄-NH] y - (CH₂CH₂CH₂CH₂O) x - (CH₂) ₄-NH₂ (I),
in which x is 1 to 150 and y is 1 or 2, and a process for the preparation of these compounds, in which hydroxy- (poly-n-butoxy) butanols of the general formula II
HO- (CH₂CH₂CH₂CH₂O) x - (CH₂) ₄-OH (II),
in which x denotes 1 to 150, with 1.01 to 300 molar equivalents of ammonia per hydroxyl group in the presence of a hydrogenation / dehydrogenation catalyst and hydrogen at temperatures of 150 to 300 ° C. and pressures of 20 to 400 bar.

EP19890114498 1988-08-10 1989-08-05 Amino-mono or amino-di[(poly-n-butoxy)-n-butyl amino]-(poly-n-butoxy)-n-butyl amines Withdrawn EP0354501A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3827119A DE3827119A1 (en) 1988-08-10 1988-08-10 AMINO-MONO- OR -DI (POLY-N-BUTOXY) -N-BUTYLAMINO - (POLY-N-BUTOXY) -N-BUTYLAMINE
DE3827119 1988-08-10

Publications (2)

Publication Number Publication Date
EP0354501A2 EP0354501A2 (en) 1990-02-14
EP0354501A3 true EP0354501A3 (en) 1991-08-07

Family

ID=6360581

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890114498 Withdrawn EP0354501A3 (en) 1988-08-10 1989-08-05 Amino-mono or amino-di[(poly-n-butoxy)-n-butyl amino]-(poly-n-butoxy)-n-butyl amines

Country Status (4)

Country Link
US (1) US4973761A (en)
EP (1) EP0354501A3 (en)
JP (1) JPH02104566A (en)
DE (1) DE3827119A1 (en)

Families Citing this family (22)

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Publication number Priority date Publication date Assignee Title
GB9007048D0 (en) * 1990-03-29 1990-05-30 Bp Chem Int Ltd Lubricating oil additives and their preparation
US5436351A (en) * 1993-08-27 1995-07-25 Huntsman Corporation Imidazolidone polyetheramide surfactant
US5422042A (en) * 1993-11-19 1995-06-06 Huntsman Corporation Imidazolidone polyetheramine strength enhancing additives of epoxy resin systems
US5817593A (en) * 1995-06-02 1998-10-06 The Dow Chemical Company Catalyst and process for producing amines
JPH11514401A (en) * 1995-10-04 1999-12-07 ザ ダウ ケミカル カンパニー Amine-terminated polyether and method for producing the same
US6838407B2 (en) 2001-11-30 2005-01-04 Lord Corporation Room temperature curable fluoropolymer coating
US6777026B2 (en) * 2002-10-07 2004-08-17 Lord Corporation Flexible emissive coatings for elastomer substrates
US6844412B2 (en) * 2002-07-25 2005-01-18 Lord Corporation Ambient cured coatings and coated rubber products therefrom
KR101237170B1 (en) 2004-05-13 2013-02-25 헌츠만 페트로케미칼 엘엘씨 Comb-like polyetheralkanolamines in inks
US20070265396A1 (en) 2004-11-05 2007-11-15 Srimannarayana Kakarala Thermoplastic polyolefin compositions having improved melt viscosity and methods of making the same
US20070276094A1 (en) * 2004-11-05 2007-11-29 Srimannarayana Kakarala Thermoplastic polyolefin compositions having improved adhesion to polymer foams and/or coatings and methods of making and using the same
DE102005029932A1 (en) * 2005-06-28 2007-01-11 Clariant Produkte (Deutschland) Gmbh Process for the preparation of polyetheramines
MX2009006053A (en) * 2006-12-06 2009-06-16 Clariant Finance Bvi Ltd Process for preparing polyetheramines.
CA2913375A1 (en) 2007-10-19 2009-04-30 Lord Corporation Suspension system for aircraft auxiliary power unit with elastomeric member
JP5251883B2 (en) * 2007-10-31 2013-07-31 宇部興産株式会社 Polyether polyamide elastomer and laminate using the same
US10208168B2 (en) 2011-10-25 2019-02-19 Kraton Polymers U.S. Llc Polyoxyalkyleneamine modified sulfonated block copolymers, their preparation and their use
CA2855758C (en) 2011-12-29 2020-04-28 Chevron Oronite Company Llc Functionalized olefin copolymers with monoamine terminated polyether and lubricating oil compositions
CN108135185B (en) 2016-03-08 2024-05-17 银都拉玛投资氧化物有限责任公司 Concentrated low viscosity agricultural formulations
CN107754813B (en) 2016-08-18 2019-09-20 万华化学集团股份有限公司 A kind of loaded catalyst and preparation method thereof for polyetheramine synthesis
US20180171258A1 (en) 2016-12-16 2018-06-21 Afton Chemical Corporation Multi-Functional Olefin Copolymers and Lubricating Compositions Containing Same
US10513668B2 (en) 2017-10-25 2019-12-24 Afton Chemical Corporation Dispersant viscosity index improvers to enhance wear protection in engine oils
US11098262B2 (en) 2018-04-25 2021-08-24 Afton Chemical Corporation Multifunctional branched polymers with improved low-temperature performance

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1134132A (en) * 1965-10-14 1968-11-20 Minnesota Mining & Mfg Polyether polyamines, their production and products derived therefrom

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3824220A (en) * 1963-06-24 1974-07-16 Minnesota Mining & Mfg Polycationically active polymers
US3824219A (en) * 1963-06-24 1974-07-16 Minnesota Mining & Mfg Process for preparing polycationically active polymers of tetrahydrofuran
US3352916A (en) * 1964-04-15 1967-11-14 Atlas Chem Ind Aminated polyoxyalkylene fatty amines
GB1129657A (en) * 1964-12-02 1968-10-09 Asahi Chemical Ind Method for preparing copolymers
US3824197A (en) * 1966-02-10 1974-07-16 Minnesota Mining & Mfg Process for preparing poly-cationically active polymers from preformed polymers
US3824198A (en) * 1966-02-10 1974-07-16 Minnesota Mining & Mfg Process for reacting active hydrogen containing compounds with polycationically active polymers
US4181682A (en) * 1978-01-09 1980-01-01 Texaco Development Corp. Aminated propoxylated polybutanediols
US4618717A (en) * 1984-09-17 1986-10-21 Texaco Inc. Catalytic process for the production of primary amines from oxyethylene glycol monoalkyl ethers
US4766245A (en) * 1985-03-01 1988-08-23 Texaco Inc. Process for the preparation of polyoxyalkylene polyamines
US4847417A (en) * 1987-08-03 1989-07-11 Texaco Inc. Bis(diaminopolyalkoxy)-N-alkylamines by amination of hydroxyl-containing tertiary amines

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1134132A (en) * 1965-10-14 1968-11-20 Minnesota Mining & Mfg Polyether polyamines, their production and products derived therefrom

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 108, no. 6440, 04 Januar 1988 Columbus, Ohio, USA: DATABASE (Host:STN) Y.YOKOTA et al.: "Catalysts for manufacture of .,& JP-A-62 149 646 (03.07.1987)" ref. no. 133825T *
CHEMICAL ABSTRACTS, vol. 72, no. 4404, 29 Juni 1970 Columbus, Ohio, USA H.KOBAYASHI et al.: "Amination of alpha, omega ; & JP-B-45 007 553(16.03.1970)" Seite 27; ref. no. 133547S *

Also Published As

Publication number Publication date
JPH02104566A (en) 1990-04-17
DE3827119A1 (en) 1990-02-15
EP0354501A2 (en) 1990-02-14
US4973761A (en) 1990-11-27

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